rs373653682
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(GTGCTGGACGGTGTCCCT;GTGCTGGACGGTGTCCCT) | 0 | common in clinvar |
(TGTGCTGGACGGTGTCCC;TGTGCTGGACGGTGTCCC) | 0 | common in clinvar |
Make rs373653682(-;-) |
Make rs373653682(-;TGTGCTGGACGGTGTCCC) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 7961868 |
Gene | PARK7 |
is a | snp |
is | mentioned by |
dbSNP | rs373653682 |
dbSNP (classic) | rs373653682 |
ClinGen | rs373653682 |
ebi | rs373653682 |
HLI | rs373653682 |
Exac | rs373653682 |
Gnomad | rs373653682 |
Varsome | rs373653682 |
LitVar | rs373653682 |
Map | rs373653682 |
PheGenI | rs373653682 |
Biobank | rs373653682 |
1000 genomes | rs373653682 |
hgdp | rs373653682 |
ensembl | rs373653682 |
geneview | rs373653682 |
scholar | rs373653682 |
rs373653682 | |
pharmgkb | rs373653682 |
gwascentral | rs373653682 |
openSNP | rs373653682 |
23andMe | rs373653682 |
SNPshot | rs373653682 |
SNPdbe | rs373653682 |
MSV3d | rs373653682 |
GWAS Ctlg | rs373653682 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | |
Alt | |
Reference | Rs373653682(GTGCTGGACGGTGTCCCT;GTGCTGGACGGTGTCCCT) |
Significance | Pathogenic |
Disease | Parkinson disease 7 |
Variation | info |
Gene | PARK7 |
CLNDBN | Parkinson disease 7 |
Reversed | 0 |
HGVS | NC_000001.11:g.7961868_7961885dup18 |
CLNSRC | ClinVar |
CLNACC | RCV000007484.1, |